Primary Site >> Stomach Cancer
Gene >> FLNA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364551:154364551(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs374295965 |
| CDS Mutation | c.1997C>T |
| AA Mutation | p.Ala666Val(p.A666V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154348944:154348944(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.7849T>C |
| AA Mutation | p.Ser2617Pro(p.S2617P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154361328:154361328(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3187G>A |
| AA Mutation | p.Ala1063Thr(p.A1063T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154365429:154365429(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782539251 |
| CDS Mutation | c.1487G>A |
| AA Mutation | p.Arg496Gln(p.R496Q) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154358993:154358993(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782276039 |
| CDS Mutation | c.4465G>A |
| AA Mutation | p.Gly1489Arg(p.G1489R) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154354945:154354945(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5097C>A |
| AA Mutation | p.Asp1699Glu(p.D1699E) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154353196:154353196(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6031T>C |
| AA Mutation | p.Phe2011Leu(p.F2011L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154352198:154352198(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6752C>T |
| AA Mutation | p.Ala2251Val(p.A2251V) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154357470:154357470(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4909G>A |
| AA Mutation | p.Val1637Met(p.V1637M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154365218:154365218(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782067087 |
| CDS Mutation | c.1609G>A |
| AA Mutation | p.Val537Met(p.V537M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 11 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154371203:154371203(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782034946 |
| CDS Mutation | c.43G>A |
| AA Mutation | p.Ala15Thr(p.A15T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 12 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154367697:154367697(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782425251 |
| CDS Mutation | c.664G>A |
| AA Mutation | p.Val222Ile(p.V222I) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 13 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364152:154364152(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2150G>A |
| AA Mutation | p.Cys717Tyr(p.C717Y) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 14 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154365247:154365247(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782450368 |
| CDS Mutation | c.1580G>A |
| AA Mutation | p.Arg527His(p.R527H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 15 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154353437:154353437(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.5881T>C |
| AA Mutation | p.Ser1961Pro(p.S1961P) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 16 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154360317:154360317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.3478G>A |
| AA Mutation | p.Ala1160Thr(p.A1160T) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 17 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364045:154364045(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.2257A>G |
| AA Mutation | p.Ser753Gly(p.S753G) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 18 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154354416:154354416(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5381T>C |
| AA Mutation | p.Val1794Ala(p.V1794A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 19 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154349747:154349747(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7454T>C |
| AA Mutation | p.Val2485Ala(p.V2485A) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 20 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364644:154364644(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.1904A>G |
| AA Mutation | p.Tyr635Cys(p.Y635C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 21 |
| Mutation Consequence | missense_variant;splice_region_variant |
| Transcription ID | ENST00000369850 |
| Start | 154367844:154367844(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs28935469 |
| CDS Mutation | c.620C>T |
| AA Mutation | p.Pro207Leu(p.P207L) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 22 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154360248:154360248(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3547G>A |
| AA Mutation | p.Val1183Met(p.V1183M) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 23 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364553:154364553(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368889011 |
| CDS Mutation | c.1995C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 24 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154348873:154348873(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7920C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 25 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154357576:154357576(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4803C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 26 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364625:154364625(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs80338841 |
| CDS Mutation | c.1923C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 27 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154353351:154353351(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs372351673 |
| CDS Mutation | c.5967G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 28 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154353101:154353101(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782443621 |
| CDS Mutation | c.6126G>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 29 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154351587:154351587(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7017C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 30 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154366094:154366094(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781810182 |
| CDS Mutation | c.1359C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 31 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154349686:154349686(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.7515C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 32 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154362707:154362707(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs781789768 |
| CDS Mutation | c.2358C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 33 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154366628:154366628(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.999C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 34 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154359739:154359739(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782259468 |
| CDS Mutation | c.3972C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 35 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154362776:154362776(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2289G>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 36 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154360510:154360510(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs199530601;rs786205187 |
| CDS Mutation | c.3285C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 37 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154366369:154366369(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs368227790 |
| CDS Mutation | c.1167C>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 38 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154358519:154358519(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.4524C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 39 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154353014:154353014(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | null |
| CDS Mutation | c.6213T>C |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 40 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154354849:154354849(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5193G>T |
| Mutation Classification | Silent |
| Feature Type | Transcript |
| ID | 41 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369850 |
| Start | 154354896:154354896(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | null |
| CDS Mutation | c.5146delC |
| AA Mutation | p.Gln1716SerfsTer23(p.Q1716Sfs*23) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 42 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369850 |
| Start | 154348893:154348893(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.7900delG |
| AA Mutation | p.Asp2634ThrfsTer71(p.D2634Tfs*71) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 43 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369850 |
| Start | 154362456:154362456(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.2527delG |
| AA Mutation | p.Ala843LeufsTer33(p.A843Lfs*33) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 44 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369850 |
| Start | 154361323:154361323(version: GRCh38) |
| Mutation Type | DEL |
| dbSNP_RS | novel |
| CDS Mutation | c.3192delC |
| AA Mutation | p.Thr1065ProfsTer6(p.T1065Pfs*6) |
| Mutation Classification | Frame_Shift_Del |
| Feature Type | Transcript |
| ID | 45 |
| Mutation Consequence | stop_gained |
| Transcription ID | ENST00000369850 |
| Start | 154359738:154359738(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3973G>T |
| AA Mutation | p.Glu1325Ter(p.E1325*) |
| Mutation Classification | Nonsense_Mutation |
| Feature Type | Transcript |
| ID | 46 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369850 |
| Start | 154362455:154362456(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | rs782312089 |
| CDS Mutation | c.2527dupG |
| AA Mutation | p.Ala843GlyfsTer12(p.A843Gfs*12) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |
| ID | 47 |
| Mutation Consequence | frameshift_variant |
| Transcription ID | ENST00000369850 |
| Start | 154366211:154366212(version: GRCh38) |
| Mutation Type | INS |
| dbSNP_RS | novel |
| CDS Mutation | c.1241dupG |
| AA Mutation | p.Glu415ArgfsTer65(p.E415Rfs*65) |
| Mutation Classification | Frame_Shift_Ins |
| Feature Type | Transcript |